The offensive nature of maternal aggression in mice: Effects of fluprazine hydrochloride

The phenylpiperazine fluprazine hydrochloride was used to test the hypothesis that maternal aggression in laboratory mice reflects offensive motivation. Lactating females (n = 8 per condition) tested for aggression following drug treatment (1.0 mg/kg and 5.0 mg/kg of fluprasine) were significantly less aggressive than saline controls according to all measures used. The findings support the hypothesis that maternal aggression is offensive in nature, and provide no evidence that maternal attack is a mixture of offensive and defensive tendencies.     

Analysis of the targets and tactics of conspecific attack and predatory attack in northern grasshopper mice onychomys leucogaster

Comparisons of tactics of fighting between species are often difficult to make since the body targets attacked may differ. Thus it becomes difficult to assess whether differences in fighting tactics are due to species-specific differences in the tactics themselves or due to the different targets attacked. A solution to this problem is to analyse the tactics of a species that attacks different targets under different circumstances. In this way, differences in tactics can be more readily attributed to differences in targets. In this study, resident male northern grasshopper mice (Onychomys leucogaster) were tested against intruding male conspecifics and against laboratory mice (Mus musculus domesticus). Conspecifics were mainly bitten on the lower dorsum, whereas prey were bitten and killed by bites to the nape of the neck. Therefore, it was possible to analyze the tactics of attack by grasshopper mice when attacking different body targets. For example, in order to defend the lower dorsum and the nape, both intruding conspecifics and prey adopted an upright defensive posture. Resident grasshopper mice used the lateral attack tactic to gain access to the lower flanks but not the nape. This illustrates that the lateral attack tactic is not merely a tactic suitable for overcoming the upright defense tactic, but is used in this context only when the target attacked is on the opponent's posterior dorsum. Such withinpecies comparison enables the identification of the contextual rules which govern the use of fighting tactics. © 1992 Wiley-Liss, Inc.     

Effects of Eltoprazine Hydrochloride on Predatory Behavior in Rats

Treatment of rats with the potent antiaggressive compound eltoprazine hydrochloride (1.0 & 2.0 mg/kg) slowed both predatory attack and killing of frogs. These results demonstrate a specific predation-inhibiting action of the drug which is not obscured by the elements of conspecific aggression seen during muricide. Unlike the closely related compound fluprazine, eltoprazine increased both attack and kill latencies implying that the effects of the two drugs on predation are mediated by at least somewhat distinct drug actions. It is further suggested that eltoprazine may be more specifically antiaggressive in its actions than related phenylpiperazine compounds.

     

Food deprivation: Effects on the predatory behavior of southern grasshopper mice (Onychomys torridus)

The southern grasshopper mouse (Onychomys torridus) is a predatory and aggressive rodent native to the semi-arid scrub deserts of the southwestern United States and northern Mexico. Its natural diet consists primarily of arthropods and small vertebrates. In this study, we have evaluated the effects of food deprivation on the predatory behavior of adult male and female grasshopper mice to crickets (Acheta domesticus) and laboratory mice (Mus musculus). Subjects that were food-deprived for 48 hours spent more time eating dead but not living crickets than did controls that were provided free access to laboratory chow. There were no sex differences in the predatory behavior of grasshopper mice to living or dead crickets. Food deprivation also influenced the predatory behavior of grasshopper mice toward laboratory mice. With laboratory chow available ad lib, 6 of 43 (14%) male and 22 of 45 (49%) female grasshopper mice killed and ate laboratory mice within 48 hours of pairing. When deprived of food for 48 hours, 16 of 36 (44%) males and 15 of 19 (79%) females that did not kill in the previous experiment killed and ate laboratory mice. We concluded that food deprivation and type of prey are two variables which influence the frequency and intensity of predatory behaviors of grasshopper mice.     

Hearing in two cricetid rodents: wood rat (Neotoma floridana) and grasshopper mouse (Onychomys leucogaster)

The audiograms of two wood rats and three grasshopper mice were determined with a conditioned avoidance procedure. The wood rats were able to hear tones from 940 Hz to 56 kHz at a level of 60 dB (SPL), with their best sensitivity of -3 dB occurring at 8 kHz. The hearing of the grasshopper mice ranged from 1.85 kHz to 69 kHz at 60 dB (SPL), with their best sensitivity of 9 dB also occurring at 8 kHz. These results support the relation between interaural distance and high-frequency hearing and between high- and low-frequency hearing. The inability of the grasshopper mouse to hear low frequencies as well as other desert rodents such as kangaroo rats and gerbils demonstrates that not all rodents found in deserts have developed good low-frequency hearing. The degree to which general and specific selective pressures have played a role in the evolution of rodent hearing is discussed.     

Sound localization in a predatory rodent, the northern grasshopper mouse (Onychomys leucogaster)

A comparison of the ability of mammals to localize sound revealed that among the animals examined to date, none of the rodents have been able to localize as accurately as the carnivores. Because all of these rodents are prey animals, the question arises as to whether their poor localization acuity is a phyletic trait of Rodentia or whether it is a trait common to prey species that may be under less selective pressure than predators to localize sound accurately. To answer this question, sound localization acuity was determined in a species that is both predatory and a rodent, the northern grasshopper mouse. Localization thresholds for a single 100-ms noise burst were determined for three grasshopper mice using a conditioned avoidance procedure. Their 50% discrimination threshold of 19 degrees is larger than that of any of the previously tested carnivores and well within the range of other rodents. However, calculations of the binaural sound localization cues available to rodents (based on their head size) suggest that the grasshopper mouse may make more efficient use of the available locus cues than other rodents. Thus, although the grasshopper mouse cannot localize as accurately as carnivores, it appears to be more accurate than predicted for a nonpredatory rodent of its size.     

Partial kindling and emotional bias in the cat: lasting aftereffects of partial kindling of the ventral hippocampus. I. Behavioral changes

Repeated electrical evocation of afterdischarges in the perforant-path ventral hippocampal system of the cat produces lasting changes in species characteristic behavioral responses to environmental threat. After 7 to 12 afterdischarges, cats showed greatly enhanced defensive (withdrawal) responses to rats, and mildly enhanced defensive responses toward mice. Measures of predatory attack which negatively correlate with withdrawal from rats were also changed in a direction consistent with the increase in withdrawal tendency. There was little effect of afterdischarges on the same parameters of attack on mice. Thus the stimulation seemed to attenuate predatory aggression by increasing defensive sensitivity to the threat posed by prey self-defense, and not by reducing predatory motivation per se. The change in defensiveness was not restricted to the predatory test situation, however. Tests of defensive response to conspecific threat vocalizations revealed an increased defensive responding to this stimulus as well. On the other hand, there was no change in social responsiveness shown toward a highly familiar human. Given the sudden onset (1 hr to 24 hr after the last afterdischarge), the long-lasting nature of the change (30-60 days) which persisted in the absence of seizures, and the generality of expression of the behavioral change, it was concluded that the afterdischarges produced an interictally maintained alteration in a defensive personality characteristic of the cats.     

Some fear-potentiating effects of fluprazine hydrochloride in mice

The fear-potentiating effects of fluprazine hydrochloride were explored in a series of five experiments. The drug was found to strongly inhibit entry into a novel open field, exploration of a complex maze, or approach to a novel object placed in the animal's home cage. Time sampling techniques were used to assess drug effects on frequencies of immobility, activity, and grooming and rearing responses prior to and for 70 min after footshock. There were no group differences during the 10 min immediately following shock but the groups diverged steadily in immobility, activity, and grooming for the remainder of the observations. Post-shock activity and grooming responses increased steadily towards baseline values among control mice but remained at low levels or declined among drug-treated mice. Immobility responses declined steadily among control mice but increased substantially among the fluprazine-treated mice throughout post-shock observations. Pairs of male mice treated with fluprazine were also found to maintain greater intermouse distances in a novel linear runway than pairs of undrugged adult males, juvenile males, or male-female pairs. It is suggested that fluprazine hydrochloride both potentiates fear and alters its time course in addition to interfering in some way with normal olfactory processes.     

Effects of toxicosis on the predatory behavior of the golden hamster (Mesocricetus auratus)

The purpose of this study was to measure the effects that toxicosis had on the hamster's predatory behavior and to compare these results with those found in previous studies with grasshopper mice. A 0.15 M LiCl injection caused hamsters to develop a greater aversion and to inhibit their feeding and attack responses more frequently toward a house cricket than did a similar injection of NaCl. The added presence of an almond coating on the cricket prolonged the number of days that a hamster exhibited an aversion toward the prey and an inhibition to attack. Essentially, the inhibitory effects from toxicosis in the hamster paralleled those found with the grasshopper mouse. The differences in these inhibitory effects are attributed to inherent differences in the attack responses of the two rodents.     

Effects of poisoning on predatory and ingestive behavior toward artificial prey in rats (Rattus norvegicus)

Ingestion of novel prey by vertebrate predators that is followed by illness typically decreases the predators' eating the prey more readily than their pursuing or killing it. We used artificial prey-food items (rolling ball bearings that predicted food pellets) to model and extend this finding in laboratory rats. During daily experimental sessions presentations of a novel bearing-food combination were intermixed with presentations of a familiar bearing-food combination. The poisoned animals received lithium chloride injections after each session. Experiment 1a showed that: (a) Poisoning markedly decreased ingestion of the novel food without decreasing the frequency of contact (nose, seize, carry, or chew) with the novel bearing predicting that food. (b) However, poisoning did significantly decrease the average duration of contact with the novel bearing. (c) Poisoning did not decrease behavior toward the familiar food and bearing. Experiment 1b showed that after moderate exposure to pairings of the novel food and bearing, poisoning decreased behavior toward both novel and familiar food and bearings. The results indicate that important aspects of predation can be simulated and examined in the laboratory by using artificial prey-food items. These results also support the conclusions that predatory behavior and ingestion reflect separable modes of behavior and that the presence of novel prey interferes with the generalization of poisoning effects to familiar prey.     

Effects of some physiological and pharmacological manipulations on shock- facilitated mouse killing by onychomys leucogaster (Northern grasshopper mouse)

Onychomys leucogaster (northern grasshopper mice) were induced to kill mice with response-contingent shock, and the effects of several physiological, pharmacological, and endocrinological variables were assessed. Lesions of the septum facilitated mouse killing, while lesions of the amygdala abolished spontaneous mouse killing and delayed shock-facilitated killing. Chlorpromazine (2.5–5 mg/kg) and chlordiazepoxide (5–10 mg/kg) facilitated mouse killing on postdrug trials but did not affect killing when the animals were drugged. Adrenalectomy, castration, and castration adrenalectomy did not alter the frequency of kill nor were sex-related differences in killing noted. These results were compared to those found by others studying the effects of lesions and drugs on mouse killing by rats.     

Behaviors of Swiss-Webster and C57/BL/6N sin mice in a fear/defense test battery

When confronted by an approaching threat stimulus (experimenter or laboratory rat), Swiss-Webster mice show initial flight, followed by freezing and defensive vocalization and biting, the latter only when escape is blocked. These defense patterns resemble those of the wild rat, suggesting that mice of this strain do not show the reductions in flight and defensive threat/attack that are typical of laboratory rats. C57/BL/6N Sin strain mice showed fewer avoidances to an approaching predator, as well as reduced vocalization and defensive biting, a pattern more similar to that of laboratory rats. As with rats, female mice appeared to be more defensive to a predator. They showed greater reactivity to dorsal contact and more frequent defensive biting and jump attacks than males of the same strains. These patterns of defensive behaviors suggest that, although strain differences in defense are substantial, laboratory mice are suitable for, and may offer several advantages in, the study of the genetic, endocrine, and pharmacological basis of antipredator defense. © 1995 Wiley-Liss, Inc.     

Effects of Fluprazine Hydrochloride on Three Aversively Motivated Tasks

The Psychological Record - Treatment with 8.0 mg/kg fluprazine hydrochloride had no effect on the acquisition of a step-down avoidance response but retarded its extinction. The drug also impaired...     

Reinforcement and Inhibition of Eyelid Reflexes

Taste preferences, as measured in 48-hour, Richter-type drinking tests (test solution opposite distilled water), were determined for northern grasshopper mice (Onychomys leucogaster, ssp. breviauritus). The Ss were nine males and nine females which were individually housed within an environmental chamber. The test solutions were prepared from five sugars (fructose, glucose, lactose, maltose, sucrose), three salts (magnesium sulfate, potassium chloride, sodium chloride), and two acids (citric acid and hydrochloric acid). In randomly assigned order, each sugar and each salt solution was presented at five molar concentrations, and each acid was paired with distilled water at six levels of pH. Strong drinking preferences were shown for all concentrations of the sugars above .05?.10 M, and sugars ranked in order of preference as follows: Maltose = sucrose > glucose = fructose > lactose. Preferences were also shown for hypotonic concentrations of NaCl. The other salts and both acids, however, were indifferently preferred at low concentrations and were rejected at the higher concentrations. Taste preferences by grasshopper mice for these chemicals were similar to those exhibited by Mongolian gerbils tested with the same items. The similar patterns of preference shown by New World cricetid rodents (grasshopper mice) and Old World cricetid rodents (gerbils) suggest that conclusions concerning disparity in taste sensibilities among animal forms may be premature.     

Relationship between attack and feeding in the insect predatory behavior of grasshopper mice

In grasshopper mice, the consequences of feeding and state of hunger affect the predatory attack to a limited extent. The purpose of this study was: (1) to establish other ways that attack and feeding were connected besides the two effects already mentioned; and (2) to determine if caching of dead prey could account for the limited connection between attack and feeding. Experiment 1 showed that attack and feeding were connected as part of a reaction chain. Experiment 2 showed that both shared a common maturational process despite the fact that each response achieved an improved efficiency in a different way. Experiment 3 showed that caching prey was not correlated with the killing of a prey and thus could not account for the limited connection between attack and feeding. It is proposed that a highly canalized attack response specifically buffered against the effects of feeding and hunger plays an important role in the mouse's carnivorous life style.     

The organization of play fighting in the grasshopper mouse (Onychomys leucogaster): Mixing predatory and sociosexual targets and tactics

The body targets contacted, the type of contact made, and the patterns of defense and counterattack elicited by those attacks are examined in the play fighting of captive male and female pairs of grasshopper mice. The nape was the most frequently contacted body target, irrespective of the type of contact made, be it nosing, allogrooming, biting, or striking with a forepaw. The types of defense varied with both body area contacted and type of attack performed. Based on the topography and pattern of contact, it was concluded that grasshopper mice, as is the case for many other muroid rodents, primarily attack and defend targets otherwise contacted during precopulatory encounters. However, grasshopper mice, which are obligate carnivores, also attack and defend predatory targets, although less frequently than sociosexual targets. Surprisingly, predatory attacks were more likely to be counterattacked with predatory attacks, whereas sociosexual attacks were more likely to be counterattacked with sociosexual attacks. Conspecific aggression involves bites directed at the face, lower flanks, and dorsum. Neither the biting of these areas nor the tactics of attack and defense usually associated with such bites were observed during the juvenile interactions. There were no sex differences in either frequency or patterns of attack and defense in play fighting. The data presented for grasshopper mice shed light on the issue of mixing behavior patterns from multiple functional systems during play. Aggr. Behav. 26:319–334, 2000. © 2000 Wiley‐Liss, Inc.     

Effects of D- and L-amphetamine on the predatory behavior of Southern grasshopper mice,onychomys torridus

Adult male and female southern grasshopper mice (Onychomys torridus) were tested for predatory aggression toward cricket prey 1 hr after single injections of d-amphetamine (1 or 10 mg/kg) or 1-amphetamine (1 or 10 mg/kg). At the lower dose, d-amphetamine decreased feeding behaviors, while I-amphetamine altered attack-related behaviors. At the higher dose, both stereoisomers appeared to be equipotent in significantly decreasing 5 measures of predatory aggression. These results suggest that brain dopamine and norepinephrine play important roles in the regulation of predatory aggression of Onychomys torridus.     

Memory of captured prey in three web spiders (Araneae: Araneidae, Linyphiidae, Tetragnathidae)

We gave three web spiders, Argiope argentata (Araneidae), Nephila clavipes (Tetragnathidae) and Neriene peltata (Linyphiidae), large and small prey which we then removed from the spiders’ webs. Following prey removal the spiders searched by walking around the web and pulling on its threads for several minutes, stopping when allowed to find the prey. Spiders that captured larger prey searched for longer. Searching behaviour was different from the spiders’ responses to disturbance and did not appear to be elicited by proximal cues. Instead, the spiders formed memories of captured prey that included details about prey size and freshness. Received: 3 March 2000 / Accepted after revision: 24 July 2000     

Some aspects of predatory behavior

Predatory behavior is conceived of as a loose chain of responses including searching for relevant stimuli, hunting or chasing potential prey, capturing or attacking prey, and killing and feeding on prey. These aspects, which may occur independently, are described and discussed separately with an emphasis on mammalian species of carnivores. Particular attention is paid to opportunism in prey selection, specific searching images with their possible antecedents, the role of hunger in prey attack, and the phenomenon of surplus killing. Finally a discussion of mouse killing by rats attempts to show similarities between this and other more traditional examples of predation.     

Prey positions as consumers' behavioural patterns: Exploratory evidence from an fMRI study

The present article reviews some of the tenets of the Consolidated Model of Financial Predation (CMFP). The CMFP is used to explain how investors behave as either predators or prey in the financial markets, for example, during the 2008 predatory‐mortgages crisis. The article tests one of its key assumptions: that is, that people adopt different levels of prey positions. In the last four years, a number of articles have been published on the CMFP, which states that people adopt either a predator or a prey position (PPP), or else a mixture of both. The model has emerged as a result of a five‐year study and has found various applications, in particular, in the field of behavioural finance. According to this model, consumers of financial products tend to position themselves as either predators or prey. In the latter case, this causes them to judge the relationship in negative terms and to experience it as less rewarding, if not punishing altogether. This has two effects: first, perceived predation tends to gain in power and second, purchasing decisions may not be optimal. Results from an exploratory functional magnetic resonance imaging (fMRI) study aimed at generating prey positions in minimal stress conditions are presented; they show that there is a significant difference between at least two prey positions, labelled “known predator–prey position” (KPPP) and “unknown predator–prey position” (UPPP). This means that consumers of financial products could potentially face two levels of apprehension (perceived predation): a high one under uncertainty and a lower one when conditions are volatile. Copyright © 2016 John Wiley & Sons, Ltd.